510(k) K934123 ยท DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
STOPCOCK (ONE-PORT MANIFOLD)
| Applicant | Merit Medical Systems, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Nov 23, 1993 |
| Received | Aug 25, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934123
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 6, 2003 | Merit Medical Systems, Inc Custom Angiographic Kit. Terminated |
DQO | None listed |
| Mar 6, 2003 | Merit Medical Systems, Inc Custom Angiographic Kit Terminated |
DQO | None listed |
| Mar 6, 2003 | Merit Medical Systems, Inc Custom Angiographic Kit Terminated |
DQO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.